Gwen Murphy, Neal D. Freedman, Christian C. Abnet, Demetrius Albanes, Amanda J. Cross, Wen-Yi Huang, Jill Koshiol, Katherine McGlynn, Dominick Parisi, Satu Männistö, Stephanie J. Weinstein, Tim Waterboer, Julia Butt
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We used a multiplex panel to assess whether seropositivity to <i>Helicobacter (H.) hepaticus</i> or <i>H. bilis</i> proteins was associated with the development of hepatobiliary cancers in the Finnish Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study, and US-based Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO).</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We included 62 biliary and 121 liver cancers, and 190 age-matched controls from ATBC and 74 biliary and 105 liver cancers, and 364 age- and sex-matched controls from PLCO. Seropositivity to 14 <i>H. hepaticus</i> and <i>H. bilis</i> antigens was measured using a multiplex assay. Odds ratios (ORs) and 95% confidence intervals (CIs) were adjusted for major hepatobiliary cancer risk factors and <i>Helicobacter pylori</i> serostatus.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Seropositivity to the <i>H</i>. <i>bilis antigen,</i> P167D, was associated with more than a twofold higher risk of liver cancer (OR: 2.38; 95% CI: 1.06, 5.36) and seropositivity to the <i>H</i>. <i>hepaticus</i> antigens HH0407 or HH1201, or <i>H. bilis</i> antigen, HRAG 01470 were associated with higher risk of biliary cancer (OR: 5.01; 95% CI: 1.53, 16.40; OR: 2.40; 95% CI: 1.00, 5.76; OR: 3.27; 95% CI: 1.14, 9.34, respectively) within PLCO. No associations for any of the <i>H</i>. <i>hepaticus or H</i>. <i>bilis</i> antigens were noted for liver or biliary cancers within ATBC.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Further investigations in cohort studies should examine the role of <i>Helicobacter</i> spp. in the etiology of liver and biliary cancers.</p>\n </section>\n </div>","PeriodicalId":13223,"journal":{"name":"Helicobacter","volume":"29 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/hel.13053","citationCount":"0","resultStr":"{\"title\":\"Helicobacter hepaticus and Helicobacter bilis in liver and biliary cancers from ATBC and PLCO\",\"authors\":\"Gwen Murphy, Neal D. Freedman, Christian C. Abnet, Demetrius Albanes, Amanda J. Cross, Wen-Yi Huang, Jill Koshiol, Katherine McGlynn, Dominick Parisi, Satu Männistö, Stephanie J. Weinstein, Tim Waterboer, Julia Butt\",\"doi\":\"10.1111/hel.13053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p><i>Helicobacter</i> species (spp.) have been detected in human bile and hepatobiliary tissue <i>Helicobacter</i> spp. promote gallstone formation and hepatobiliary tumors in laboratory studies, though it remains unclear whether <i>Helicobacter</i> spp. contribute to these cancers in humans. We used a multiplex panel to assess whether seropositivity to <i>Helicobacter (H.) hepaticus</i> or <i>H. bilis</i> proteins was associated with the development of hepatobiliary cancers in the Finnish Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study, and US-based Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>We included 62 biliary and 121 liver cancers, and 190 age-matched controls from ATBC and 74 biliary and 105 liver cancers, and 364 age- and sex-matched controls from PLCO. Seropositivity to 14 <i>H. hepaticus</i> and <i>H. bilis</i> antigens was measured using a multiplex assay. Odds ratios (ORs) and 95% confidence intervals (CIs) were adjusted for major hepatobiliary cancer risk factors and <i>Helicobacter pylori</i> serostatus.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Seropositivity to the <i>H</i>. <i>bilis antigen,</i> P167D, was associated with more than a twofold higher risk of liver cancer (OR: 2.38; 95% CI: 1.06, 5.36) and seropositivity to the <i>H</i>. <i>hepaticus</i> antigens HH0407 or HH1201, or <i>H. bilis</i> antigen, HRAG 01470 were associated with higher risk of biliary cancer (OR: 5.01; 95% CI: 1.53, 16.40; OR: 2.40; 95% CI: 1.00, 5.76; OR: 3.27; 95% CI: 1.14, 9.34, respectively) within PLCO. 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Helicobacter hepaticus and Helicobacter bilis in liver and biliary cancers from ATBC and PLCO
Background
Helicobacter species (spp.) have been detected in human bile and hepatobiliary tissue Helicobacter spp. promote gallstone formation and hepatobiliary tumors in laboratory studies, though it remains unclear whether Helicobacter spp. contribute to these cancers in humans. We used a multiplex panel to assess whether seropositivity to Helicobacter (H.) hepaticus or H. bilis proteins was associated with the development of hepatobiliary cancers in the Finnish Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study, and US-based Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO).
Methods
We included 62 biliary and 121 liver cancers, and 190 age-matched controls from ATBC and 74 biliary and 105 liver cancers, and 364 age- and sex-matched controls from PLCO. Seropositivity to 14 H. hepaticus and H. bilis antigens was measured using a multiplex assay. Odds ratios (ORs) and 95% confidence intervals (CIs) were adjusted for major hepatobiliary cancer risk factors and Helicobacter pylori serostatus.
Results
Seropositivity to the H. bilis antigen, P167D, was associated with more than a twofold higher risk of liver cancer (OR: 2.38; 95% CI: 1.06, 5.36) and seropositivity to the H. hepaticus antigens HH0407 or HH1201, or H. bilis antigen, HRAG 01470 were associated with higher risk of biliary cancer (OR: 5.01; 95% CI: 1.53, 16.40; OR: 2.40; 95% CI: 1.00, 5.76; OR: 3.27; 95% CI: 1.14, 9.34, respectively) within PLCO. No associations for any of the H. hepaticus or H. bilis antigens were noted for liver or biliary cancers within ATBC.
Conclusions
Further investigations in cohort studies should examine the role of Helicobacter spp. in the etiology of liver and biliary cancers.
期刊介绍:
Helicobacter is edited by Professor David Y Graham. The editorial and peer review process is an independent process. Whenever there is a conflict of interest, the editor and editorial board will declare their interests and affiliations. Helicobacter recognises the critical role that has been established for Helicobacter pylori in peptic ulcer, gastric adenocarcinoma, and primary gastric lymphoma. As new helicobacter species are now regularly being discovered, Helicobacter covers the entire range of helicobacter research, increasing communication among the fields of gastroenterology; microbiology; vaccine development; laboratory animal science.